FIELD: organic chemistry, heterocyclic compounds. SUBSTANCE: product: derivatives of 7-(2-aminoethyl)-benzothiazolone of the formula (I) β2 where X and Y mean independently or -O-; n = 0, 1 or 2; p, q and r mean independently 2 or 3; Z means phenyl possibly substituted with halogen, -S(O)n- or -OR1,NO2 or Z means 5- or 6- membered unsaturated heterocycle containing N or S; NH2 means hydrogen or R1-alkyl, or their pharmaceutically acceptable salts. Invention describes methods of their synthesis and pharmaceutical compositions containing thereof and also intermediate compounds for their synthesis of the formula (Va): C1-C6 where p, q and r, X, Y have indicated values and Z - phenyl optionally substituted with halogen atom, or NO2,NH2 where OR1 - H or R1--alkyl. Synthesized compounds show agonistic activity relative to C1-C6-adrenoreceptors. EFFECT: improved method of synthesis. 11 cl, 3 tbl
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